Variant #0000961022 (NC_000001.10:g.33476434_33476435insATGTGG, NM_001625.3:c.*2349_*2350insACATCC (AK2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33476434_33476435insATGTGG
DNA change (hg38) -
Published as AK2(NM_013411.5):c.691_696dupACATCC (p.T231_S232dup)
ISCN -
DB-ID AK2_000038
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AK2 NM_001625.3 -?/. - c.*2349_*2350insACATCC r.(=) p.(=)


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